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佛山市南海区2300例孕妇地中海贫血筛查结果及基因突变类型分析
引用本文:李彩凤. 佛山市南海区2300例孕妇地中海贫血筛查结果及基因突变类型分析[J]. 中国优生与遗传杂志, 2020, 0(2): 141-143
作者姓名:李彩凤
作者单位:广东省人民医院南海医院(佛山市南海区第二人民医院)妇产科
摘    要:目的 了解佛山市南海区孕妇地中海贫血筛查结果及基因突变类型,为预防地中海贫血患儿出生提供依据.方法 选取201 3年1月至201 8年12月于佛山市南海区第二人民医院行产前检查的孕妇2300例,采用全自动血细胞分析仪检测血常规,采用红细胞(RBC)脆性试验和血红蛋白(Hb)电泳试验进行地中海贫血初筛,对初筛阳性标本采用...

关 键 词:孕妇  α-地中海贫血  β-地中海贫血  基因缺失  基因突变

Analysis of thalassemia screening results and gene mutation types of 2300 pregnant women in nanhai district of foshan city
LI Cai-feng. Analysis of thalassemia screening results and gene mutation types of 2300 pregnant women in nanhai district of foshan city[J]. Chinese Journal of Birth Health & Heredity, 2020, 0(2): 141-143
Authors:LI Cai-feng
Affiliation:(Department of Obstetrics and Gynecology,Guangdong Provincial People′s Hospital of Nanhai Hospital,Second People′s Hospital,Nanhai District,Foshan City,Foshan 528251,Guangdong,China)
Abstract:Objective:To understand the screening results and gene mutation types of thalassemia among pregnant women in Nanhai District of Foshan City,and to provide evidence for preventing the birth of children with thalassemia.Methods:2300 pregnant women who underwent prenatal examination in the Second People′s Hospital of Nanhai District of Foshan City from January 2013 to December 2018 were selected.Blood routine was detected by automatic blood cell analyzer.Thalassemia was screened by erythrocyte(RBC)fragility test and hemoglobin(Hb)electrophoresis test.Polymerase chain reaction(PCR)combined with membrane hybridization was used to detect α-Thalassemia.Anemia and β-thalassemia gene detection,the results of statistical analysis.Results:750 of 2300 pregnant women with thalassemia were screened positive,the positive rate was 32.61%.211 pregnant women with thalassemia were diagnosed by gene,the positive rate was 28.13%.Among them,113 pregnant women with α-thalassemia had positive rate of 53.56%.The main gene deletion of alpha-thalassemia was--^SEA/αα deletion,with a positive rate of 66.37%,followed by-α^3.7/αα,-α^4.2/αα,with a positive rate of 20.35% and 7.96%,respectively.82 pregnant women with beta-thalassemia had positive rate of 38.86%.CD41-42 mutation was the dominant mutation in beta-thalassemia,with a positive rate of 39.02%,followed by IVS-Ⅱ-654,CD17,with a positive rate of 29.27% and 14.63%,respectively.There were 16 cases of α combined with β-thalassemia,the positive rate was 7.58%.The main mutations of α combined with β-thalassemia gene were--^SEA/αα+CD41-42,--^SEA/αα+CD28,--^SEA/αα+IVS-Ⅱ-654,-α^3.7/αα+IVS-Ⅱ-654 heterozygous mutations.The positive rates were 25.00%,12.50%,12.50% and 12.50% respectively.Conclusion:There is a certain incidence of thalassemia among pregnant women in Nanhai District of Foshan City.The main gene deletion of α-thalassemia is--^SEA/αα.The mutation of β-thalassemia gene is CD41-42.The mutation rate of heterozygous gene is on the rise.Strengthening prenatal screening and gene diagnosis of thalassemia among pregnant women in this area plays an important role in preventing the birth of fetuses with severe thalassemia.
Keywords:Pregnant woman  α-thalassemia  β-thalassemia  Gene deletion  Gene mutation
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